Supported by a growing body of evidence, radiofrequency bone tumor ablation (BTA) can help to relieve pain, protecting your quality of life.1
BTA may be an option for you if you have already received (or are currently receiving) treatment like chemotherapy or radiation, but are still experiencing pain. It also may be an option if you have exceeded your maximum radiation dose and still need relief.
Your doctor will confirm your diagnosis. If you are a good candidate for BTA, your doctor will ask you for the following information:
BTA may be performed under general anesthesia or while you are awake but sedated. Your back is numbed with a local anesthetic. Using x-ray imaging, your doctor inserts access cannulas and ablation probes and guides them to the treatment area. A high-frequency electrical current then passes through the probe, heating up and “ablating” the painful tumor.
If the ablation was performed in a weight - bearing bone, your doctor may also stabilize the area with bone cement after the ablation.
Your blood pressure and pulse will be monitored before you go home. You may feel sore or have pain in the treated area, but most people are able to return to work and normal activities within a few days.5 Timing can vary from person to person, but recent research shows pain improvement can occur in as a quickly as 3 days.1
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Serious side effects have been known to occur with the use of bone cement in surgical procedures of the spine. These include heart attack, cardiac arrest (heart stops beating), stroke, embolism (blood clot or bone cement that moves to the heart or lungs) or death. Side effects may occur beyond a year or more after the procedure.6,7
Side effects related to use of an inflatable balloon system with bone cement include wound infection, bleeding, hematoma (collection of blood outside a blood vessel), pneumothorax (collapsed lung) and anaphylaxis (severe, life-threatening allergic reaction) due to rupture of the balloon.
Please consult with your doctor for the full list of possible side effects related to the combined use of bone cement with the iVAS and iVAS Elite inflatable vertebral augmentation systems and the OmniCurve curved balloon system.8-10
The information presented is for educational purposes only. Stryker is not dispensing medical advice. Please speak to your doctor to decide what course of treatment is right for you. Only your doctor can make the medical judgment regarding which products and treatment is right for you. Any medical procedure carries certain risks and your doctor will explain all possible complications and/or side effects. Not all patients will experience the same results.
Stryker or its affiliated entities own, use or have applied for the following trademarks or service marks: AutoPlex, Dekompressor, Discmonitor, iVAS, mild, MultiGen, OmniCurve, OptaBlate, PCD, SpinePlex, SpineJack, Stryker, Venom, VertaPlex, VertaPlex HV, Verteport, and Verteport X4 Manifold. All other trademarks are trademarks of their respective owners or holders.
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